The dual burden of disease: Depression among patients with multidrug resistance tuberculosis in low-income and lower- middle-income countries: A systematic review and meta-analysis.

PLoS OneOct 13, 2026 (epub)

Agmas Wasie Abate, Assasahegn Tedla, Gashaw Mehiret Wubet et al.

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In 30 seconds

This systematic review and random-effects meta-analysis estimated depression prevalence and examined associated factors among patients with multidrug-resistant tuberculosis (MDR-TB) in low- and lower-middle-income countries. It included 23 primary studies comprising 5,734 patients. The pooled prevalence of depression was 41.89% (95% CI: 32.63-51.15; I² = 98.51%, P < 0.001). Depression was associated with female gender, financial hardship, comorbidities, greater disease severity, medication-related side effects, and perceived stigma. The authors conclude that depression is common in this population and highlight screening and psychosocial support as relevant components of care.

Key findings

  • Across 23 studies and 5,734 patients, pooled depression prevalence was 41.89% (95% CI: 32.63-51.15; I² = 98.51%, P < 0.001).
  • Perceived stigma was associated with depression (AOR = 3.58, 95% CI: 2.13-6.02).
  • Comorbidities were associated with depression (AOR = 3.72, 95% CI: 2.11-5.38).
  • Financial hardship, medication-related side effects, greater disease severity, and female gender were also significantly associated with depression.

Why it matters

Depression was common among people receiving care for MDR-TB in the settings represented, alongside clinical and social factors that may complicate treatment. Recognising this burden can help inform comprehensive assessment and support. The substantial between-study heterogeneity means the pooled estimate should be interpreted as an overall summary rather than a uniform prevalence across countries or care settings.

What to keep in mind

The pooled estimate had very high heterogeneity (I² = 98.51%), indicating substantial variation across the included studies.

Source

Published in PLoS One. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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